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成年兔淋巴祖细胞阶段B淋巴细胞生成的抑制

Suppression of B lymphopoiesis at a lymphoid progenitor stage in adult rabbits.

作者信息

Kalis Susan L, Zhai Shi-Kang, Yam Pi-Chen, Witte Pamela L, Knight Katherine L

机构信息

Department of Microbiology and Immunology, Neurobiology and Anatomy, Stritch School of Medicine, Loyola University Chicago, Maywood, IL 60153, USA.

出版信息

Int Immunol. 2007 Jun;19(6):801-11. doi: 10.1093/intimm/dxm048. Epub 2007 May 13.

Abstract

B lymphopoiesis in rabbits is robust early in ontogeny, but is arrested by 16 weeks of age at which time no proB or preB cells are found in bone marrow (BM). To determine if BM cells from adults retain B lymphopoietic potential, we transferred BM from adult green fluorescent protein (gfp) transgenic rabbits into young rabbits. We found gfp+ preB cells arising in the young recipients, indicating that BM cells from adults can differentiate into B cell precursors. We identified a population of MHCII-IL-7-binding BM cells in adults that collectively expresses Tdt, EBF and Pax5-genes known to be expressed in murine lymphoid progenitors. Upon co-culture with OP9 or OP9 delta-like 1+ stromal cells, we found that these cells both expanded in number and differentiated into B and T cell precursors, respectively, showing that early lymphoid progenitors, designated rLP for rabbit lymphoid progenitors, are present within the MHCII-IL-7-binding BM cell population. Further, IL-7 was required for rLPs to expand and differentiate into B cell precursors in vitro. The arrest of B lymphopoiesis in adults, however, is not likely due to the absence of IL-7, because the level of IL-7 transcripts was higher in BM from adults than in young rabbits. B lymphopoiesis was re-initiated in adults after sub-lethal irradiation as shown by the reappearance of B cell precursors and the presence of B cell receptor excision circles in BM. We conclude that B lymphopoiesis in adults is suppressed at a lymphoid progenitor stage (MHCII-IL-7 binding) of development.

摘要

兔子的B淋巴细胞生成在个体发育早期很活跃,但在16周龄时会停止,此时在骨髓(BM)中找不到前B细胞或前B细胞。为了确定成年兔的骨髓细胞是否保留B淋巴细胞生成潜力,我们将成年绿色荧光蛋白(gfp)转基因兔的骨髓移植到幼兔体内。我们在幼兔受体中发现了gfp +前B细胞,这表明成年兔的骨髓细胞可以分化为B细胞前体。我们在成年兔中鉴定出一群MHCII-IL-7结合骨髓细胞,它们共同表达末端脱氧核苷酸转移酶(Tdt)、早期B细胞因子(EBF)和配对盒基因(Pax5)——已知这些基因在小鼠淋巴祖细胞中表达。与OP9或OP9δ样1 +基质细胞共培养后,我们发现这些细胞数量均增加,并分别分化为B细胞和T细胞前体,这表明早期淋巴祖细胞(称为兔淋巴祖细胞rLP)存在于MHCII-IL-7结合骨髓细胞群体中。此外,IL-7是rLP在体外扩增并分化为B细胞前体所必需的。然而,成年兔B淋巴细胞生成的停止不太可能是由于缺乏IL-7,因为成年兔骨髓中IL-7转录本的水平高于幼兔。亚致死剂量照射后,成年兔的B淋巴细胞生成重新启动,骨髓中出现了B细胞前体以及B细胞受体切除环。我们得出结论,成年兔的B淋巴细胞生成在发育的淋巴祖细胞阶段(MHCII-IL-7结合)受到抑制。

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